(A) Schematic of the BS-U2 duplex used in this figure, with the positions of bulged adenosines indicated.
(B) Primer extension using a 3′ exon primer on total RNA from strains carrying reporters with adenosines bulged from the indicated positions in a grossly substituted BS-U2 duplex and either wt or mutant Prp5.
(C) Graph indicating the fold change in branching efficiency [calculated as (M+LI)/(P+M+LI)] at the −1 and 0 bulge positions as a result of Prp5 mutation.
(D, E) As (B, C), but comparing wt and mutant Prp16.